Integrated analysis of microRNA regulation and its interaction with mechanisms of epigenetic regulation in the etiology of systemic lupus erythematosus
The aim of this study was to identity in silico the relationships among microRNAs (miRNAs) and genes encoding transcription factors, ubiquitylation, DNA methylation, and histone modifications in systemic lupus erythematosus (SLE). To identify miRNA dysregulation in SLE, we used miR2Disease and Pheno...
- Autores:
-
Navarro Quiroz, Elkin
Navarro Quiroz, Roberto
Pacheco Lugo, Lisandro
Aroca Martínez, Gustavo
Gómez Escorcia, Lorena
Gonzalez Torres, Henry
Cadena Bonfanti, Andres
Marmolejo, Maria del Carmen
Sanchez, Eduardo
Villarreal Camacho, Jose Luis
Lorenzi, Hernan
Torres, Augusto
Navarro, Kelvin Fernando
Navarro Rodriguez, Pablo
Villa, Joe Luis
Fernández- Ponce, Cecilia
- Tipo de recurso:
- Fecha de publicación:
- 2019
- Institución:
- Universidad Simón Bolívar
- Repositorio:
- Repositorio Digital USB
- Idioma:
- eng
- OAI Identifier:
- oai:bonga.unisimon.edu.co:20.500.12442/3358
- Acceso en línea:
- https://hdl.handle.net/20.500.12442/3358
- Palabra clave:
- MicroRNAs
Systemic lupus erythematosus
DNA methylation
Post-translational modification
Epigenetics
Transcription factors
Gene regulation
- Rights
- License
- Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Summary: | The aim of this study was to identity in silico the relationships among microRNAs (miRNAs) and genes encoding transcription factors, ubiquitylation, DNA methylation, and histone modifications in systemic lupus erythematosus (SLE). To identify miRNA dysregulation in SLE, we used miR2Disease and PhenomiR for information about miRNAs exhibiting differential regulation in disease and other biological processes, and HMDD for information about experimentally supported human miRNA–disease association data from genetics, epigenetics, circulating miRNAs, and miRNA–target interactions. This information was incorporated into the miRNA analysis. High-throughput sequencing revealed circulating miRNAs associated with kidney damage in patients with SLE. As the main finding of our in silico analysis of miRNAs differentially expressed in SLE and their interactions with disease-susceptibility genes, post-translational modifications, and transcription factors; we highlight 226 miRNAs associated with genes and processes. Moreover, we highlight that alterations of miRNAs such as hsa-miR-30a-5p, hsa-miR-16-5p, hsa-miR-142-5p, and hsa-miR-324-3p are most commonly associated with post-translational modifications. In addition, altered miRNAs that are most frequently associated with susceptibility-related genes are hsa-miR-16-5p, hsamiR- 374a-5p, hsa-miR-34a-5p, hsa-miR-31-5p, and hsa-miR-1-3p. |
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